HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminum hydride → HCID 21880639, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | HCID 21880674 | HCID 21880674 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21880639 | HCID 21880639 | 85.1% |
Reaction Steps
A stirred solution of DIBAL (88 mL, 88 mmol, 1.0 M in cyclohexane) in THF (300 mL) was cooled to −78° C. and the intermediate from Step B (5.0 g, 17.6 mmol) was added dropwise. After complete addition, the reaction mixture was warmed to ambient temperature over 30 minutes. The reaction was then quenched by slowly adding 1N HCl (200 mL) and then DCM (400 mL) was added. The organic layer was removed and the aqueous layer was washed with DCM (4×100 mL). The combined organic layers were then washed with saturated NaCl (100 mL), dried over magnesium sulfate, filtered and the solvent removed under reduced pressure to provide 3.0 g of the title intermediate (85% yield), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250414B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-d53eea509d9d4131af5a2d1cfebe2c3e |
| Source note | uspto-grants-2007_07 |